DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MICONAZOLE 7 COMBINATION PACK
FDA Application No:
(ANDA) 076585
Active Ingredient(s):
MICONAZOLE NITRATE
Company:
G AND W LABS
Label History
Labels are not available on this site for MICONAZOLE 7 COMBINATION PACK, (ANDA) 076585
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/26/2004
000
Approval
Therapeutic Equivalents
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